Experienced CRA - Norway
IQVIA(1 day ago)
About this role
A CRA at IQVIA conducts monitoring and site management for clinical trials, ensuring adherence to study protocols, regulations, and quality standards. The role involves site visits, study documentation, and collaboration with study teams to support clinical research activities.
Required Skills
- GCP
- ICH Guidelines
- Clinical Monitoring
- Regulatory Compliance
- Trial Documentation
- Site Management
- Clinical Trials
- Communication Skills
- Time Management
- Problem Solving
About IQVIA
iqvia.comIQVIA is a leading global provider of data, technology, and advanced analytics focused on transforming healthcare and life sciences. The company empowers organizations to accelerate innovation, enhance patient outcomes, and expedite the market introduction of new treatments through comprehensive healthcare analytics and real-world evidence. With a commitment to Human Data Science, IQVIA combines its extensive expertise with innovative technology to improve health outcomes worldwide.
View more jobs at IQVIA →